Surgical Innovations Ltd recalls YelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR
Optical Trocars sterility assurance can not be guaranteed
Read the official notice →- Date
- 2023-05-24
- Country
- United States
- Brand
- Surgical Innovations
- Product
- YelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR
- Classification
- Class II
- Units
- US: MA OUS: None
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Surgical Innovations recalls
- 2022-10-05
USSurgical Innovations Ltd recalls Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures.
Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
- 2022-07-27
- US
Surgical Innovations Ltd recalls YelloPort Elite Universal Seal. For use in laparoscopic procedures.
There is the potential that YelloPort Elite Universal Seals packaging may contain small holes which may affect the sterility of the product.
FDA · DeviceSurgical Innovations LtdWorldwide distribution - US Nationwide distribution in the states of FL, IN,…Official notice →
Other drugs & medical recalls in the United States
- 2023-05-24
- US
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The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package.
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Hiossen Inc. recalls ET III Nano-HA fixture System ET NH Dental Implant Model # ET3R5010B -Intended for Dental Implant Catalog #: AET3R5010B
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Fisher Wallace Laboratories Inc. recalls Fisher Wallace Stimulator Models FW-100 and FW-200
If the batteries are installed incorrectly, the product may overheat, possibly leading to pain, discomfort, irritation, or even burns during use of the device.
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Beckman Coulter, Inc. recalls DxU 840m Iris Urine Microscopy Analyzer, Catalog Number C76947, in-vitro diagnostic device, urine analysis
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Steris Corporation recalls Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062
In the remote occurrence in which the electrical contactor component present in the drying chambers of the Reliance Vision Multi-Chamber Washer/Disinfector malfunctions, the heating elements in the drying chamber could…
FDA · DeviceSteris CorporationWorldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of:…Official notice →